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33 Cards in this Set

  • Front
  • Back
RBC casts indicate
Glomerulonephritis, ischemia, malignant HTN
WB casts indicate
Tubulointerstitial inflammation, acute pyelonephritis, transplant rejection
Fatty casts ("oval fat bodies") indicate
Nephrotic syndrome
Granular ("muddy brown") casts indicate
Acute tubular necrosis
Waxy casts indicate
Advance renal disease/CKD
Nephrotic diseases
Minimal change disease
Membranous nephropathy
Focal segmental glomerulosclerosis
Diabetic glomerulonephropathy
Amyloidosis
Nephritic diseases
IgA nephropathy (Berger's)
Acute poststreptococcal glomerulonephritis
Rapidly progressive glomerulonephritis
Alport syndrome
Nephrotic and nephritic diseases
Diffuse proliferative glomerulonephritis
Membrano-proliferative glomerulonephritis
Focal segmental glomerulosclerosis
Nephrotic
Partial glomerular sclerosis, hyalinosis
Effacement of foot processes
Most common type of nephrotic syndrome in adults and kids
Adults: focal segmental glomerulosclerosis
Kids: minimal change
Focal segmental glomerulosclerosis risk factors
HIV, heroin use, massive obesity, interferon treatment, chronic kidney disease
Nephrotic syndrome general symptoms
Massive proteinuria
Peripheral edema
Hyperlipidemia
Thromboembolic state
Increased risk of infections
Membranous nephropathy LM, IF, EM appearance
Nephrotic
LM: diffuse capillary and GBM thickening, capsular space visible
IF: granular
EM: "spike and dome" subEPIthelial deposits
SLE's nephrotic & nephritic syndrome type
Nephrotic: Membranous nephropathy
Nephritic: diffuse proliferative GN (DPGN)
Membranous nephropathy risk factors
Drugs, infections, SLE, solid tumours, or idiopathic
Minimal change disease LM, IF, EM appearance
Nephrotic
LM: no change
IF: no change
EM: foot process effacement - polyanion loss, selective albumin loss
Minimal change disease features
Selective albumin loss
Triggered by infection/immune stimulus
Most common in children
Responds to steroids
Amyloidosis stain + associations
Nephrotic
Congo red stain appears APPLE-GREEN birefringence under polarized light
Associated with chronic conditions (eg. TB, RA)
Membranoproliferative glomerulonephritis - Type I appearance + association
Nephrotic
LM: "tram-tracking" GM splitting
IF: granular
EM: subENDOthelial IC deposits
Associated with HBV, HCV
Membranoproliferative GN - Type II appearance + association
Nephrotic
Intramembranous IC deposits, "dense deposits"
Associated with C3 nephrotic factor (alternative pthwy)
Diabetic glomerulonephropathy pathophys
Nephrotic
Non-enzymatic glycosylation of GBM, efferent arteriole
GBM, arteriolar thickening
Diabetic glomerulonephropathy LM appearance
Mesangial expansion, GBM thickening, Kimmelstiel-Wilson lesion (eosinophilic nodular glomerulosclerosis)
Hyaline efferent arteriolosclerosis
Nephritic syndrome general symptoms
Hematuria
RBC casts
Azotemia
Oliguria
Hypertension
Proteinuria < 3.5 g/day
Acute poststrep glomerulonephritis LM, IF, EM characteristics
Nephritic
LM: "lumpy-bumpy" enlarged glomeruli + neurtrophils
IF: IgG, IgM, C3 deposits
EM: subEPIthelial IC humps
Acute poststrep glomerulonephritis treatment
Self-limiting
Rapidly progressive glomerulonephritis (RPGN) appearance + prognosis
Nephritic
*Crescent-shaped* lesion in glom - fibrin, C3b, macrophages, parietal cells
Poor prognosis
Diseases associated with RPGN
Goodpasture's syndrome (GBM + alveolar BM antibodies)
Wegener's granulomatosis
Microscopic polyangiitis
IF appearance in Goodpasture's
Linear IF deposits
Diffuse proliferative glomerulonephritis (DPGN) LM, IF, EM appearance
Nephritic
LM: "wire looping" capillaries
IF: granular
EM: subENDOthelial IgG with C3 deposits
DPGN causes
SLE, MPGN (membranoproliferative)
Berger's IgA nephropathy LM, IF, EM appearance
LM: mesangial proliferation
IF: IgA deposits in mesangium
EM: mesangial IC deposits
Berger's IgA nephropathy association
Henoch-Schonlein purpura
Preceded by URI, acute gastroenteritis
Alport syndrome etiology + symptoms
Type IV collagen defect --> GBM splitting (X-linked)
Nephritic glomerulonephritis, deafness, eye problems (less common)